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Active, not recruiting Not applicable Interventional

The IDEA Study (Individualized Decisions for Endocrine Therapy Alone)

ClinicalTrials.gov ID: NCT02400190

Public ClinicalTrials.gov record NCT02400190. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 31, 2026, 3:39 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will collect rates of local/regional recurrence in select patients who do not receive radiation treatment after lumpectomy surgery. These women must be postmenopausal; have hormone receptor-positive, Her2-negative tumors; have Oncotype-DX RS less than or equal to 18; and plan to receive endocrine therapy. In this way, this study seeks to collect prospective data supporting the idea that this is a population at sufficiently low risk of local/regional recurrence that omission of adjuvant radiation might be a reasonable option.

Study identification

NCT ID
NCT02400190
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Enrollment
202 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years to 69 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 27, 2015 (Actual)
Primary completion
May 2028 (Estimated)
Completion
May 2028 (Estimated)
Last update posted
Jun 3, 2026

2015 – 2028

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Stanford University Stanford California 94305 —
Yale University New Haven Connecticut 06520 —
Loyola University Medical Center Maywood Illinois 60153 —
Johns Hopkins University Baltimore Maryland — —
Harvard University Cambridge Massachusetts 02138 —
University of Michigan Ann Arbor Michigan 48109 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08901 —
Northwell Health Lake Success New York 11042 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
East Carolina University Greenville North Carolina 27853 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02400190, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 3, 2026 · Synced Oct 31, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02400190 live on ClinicalTrials.gov.

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